On-chip fabrication of calcium carbonate nanoparticles loaded with various compounds using microfluidic approach
Engineered calcium carbonate (CaCO ) particles are extensively used as drug delivery systems due to their availability, biological compatibility, biodegradability, and cost-effective production. The synthesis procedure of CaCO particles, however, suffers from poor reproducibility. Furthermore, reduc...
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Published in | Biomaterials advances Vol. 161; p. 213904 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
01.07.2024
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Subjects | |
Online Access | Get full text |
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Summary: | Engineered calcium carbonate (CaCO
) particles are extensively used as drug delivery systems due to their availability, biological compatibility, biodegradability, and cost-effective production. The synthesis procedure of CaCO
particles, however, suffers from poor reproducibility. Furthermore, reducing the size of CaCO
particles to <100 nm requires the use of additives in the reaction, which increases the total reaction time. Here we propose on-chip synthesis and loading of nanoscaled CaCO
particles using microfluidics. After the development and fabrication of a microfluidic device, we optimized the synthesis of CaCO
NPs by varying different parameters such as flow rates in the microfluidic channels, concentration of reagents, and the reaction time. To prove the versatility of the used synthesis route, we performed single and double loading of CaCO
NPs with various compounds (Doxorubicin, Cy5 or FITC conjugated with BSA, and DNA) using the same microfluidic device. Further, the on-chip loaded CaCO
NPs were used as carriers to transfer compounds to model cells. We have developed a microfluidic synthesis method that opens up a new pathway for easy on-chip fabrication of functional nanoparticles for clinical use. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2772-9508 2772-9508 |
DOI: | 10.1016/j.bioadv.2024.213904 |